For researchers

Is your paper here?

2,657 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

23 matches for Kanai M, showing the first 20.

Genome-wide association study identifies 112 new loci for body mass index in the Japanese population
Nature genetics · 2017 · PMID 28892062
12 pages+
rs77636220 rs17303831 rs4357030 rs2076463 rs2390669 rs11185092
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Nature communications · 2018 · PMID 29773799 · open access
12 pages+
rs9393800 rs707938 rs1799949 rs291269 rs1516883 rs144048300
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs6589750 rs271679 rs16942713 rs78986840 rs56411466 rs12361687
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs4766898 rs56106601 rs11202345 rs584425 rs34861762 rs4897160
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs2283159 rs79497729 rs2288450 rs78914480 rs11002805 rs80005921
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs115136484 rs117357866 rs12196128 rs12958467 rs150317881 rs1571956
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs149396823 rs17450294 rs184723794 rs201859625 rs2124616 rs34628728
Genetic analyses identify widespread sex-differential participation bias
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
rs4503596 rs6047339 rs16914670 rs35883430 rs1175109 rs6968125
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs11679380 rs11888604 rs17035776 rs17403208 rs201601284 rs28836792
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs114876144 rs145437104 rs3134988 rs7575245 rs269781 rs4741016
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs11570441 rs11656344 rs11030613 rs11769128 rs11955611 rs11991223
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs57631119 rs9380498 rs12187932 rs76181804 rs9290877 rs9594366
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans
Nature · 2023 · PMID 37587338 · open access
12 pages+
rs13177933 rs75464702 rs55955211 rs17406646 rs11085148 rs115903052
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
rs72786643 rs3091404 rs9351533 rs12886138 rs199929 rs2008551
Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults
China Kadoorie Biobank Collaborative Group
Nature communications · 2024 · PMID 39048560 · open access
12 pages+
rs10477399 rs9847595 rs6585252 rs75268076 rs62175706 rs67913572
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Nature genetics · 2026 · PMID 42509370
12 pages+
rs4802032 rs74678088 rs1977352 rs3826887 rs7332154 rs56805858
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
12 pages+
rs115686299 rs150084830 rs746708 rs34897565 rs17250932 rs13134084
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
Nature genetics · 2019 · PMID 30718926
9 pages
rs79407053 rs2908279 rs9505085 rs2844623 rs201597274 rs76550717
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs12382607 rs4328011 rs139036121 rs5933079 rs181497961 rs111410539
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194

Showing 20 of 23 · page 1 of 2

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.